A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6955790



Internal ID9717896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:98199099..98209422hg38UCSC Ensembl
Outerchr3:97917943..97928266hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810324
hg1910324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2725674, esv2725675
Supporting Variants
SamplesSSM026
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6955790
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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